FDA 510(k)

RelieVRx (Pico G3)

K-Number: K251519 · 2025-08-13

Decision Date2025-08-13

Product CodeQRA

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

RelieVRx (Pico G3) is the device name listed in this FDA 510(k) record. The listed applicant is Appliedvr. It received FDA 510(k) clearance on 2025-08-13 under 510(k) number K251519. The device is classified under product code QRA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RelieVRx (Pico G3)?

RelieVRx (Pico G3) is a medical device that received FDA 510(k) clearance on 2025-08-13. The listed applicant is Appliedvr. The 510(k) number is K251519.

When did RelieVRx (Pico G3) receive FDA 510(k) clearance?

RelieVRx (Pico G3) received FDA 510(k) clearance on 2025-08-13, under 510(k) number K251519.

Who is the listed applicant for RelieVRx (Pico G3)?

The FDA 510(k) record lists Appliedvr as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RelieVRx (Pico G3)?

The FDA product code for RelieVRx (Pico G3) is QRA.

Other records listing Appliedvr as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243417RelieVRx

Related Devices (Code: QRA)

K254004VRNTCognifisense, Inc.K243417RelieVRxAppliedvr K230814VRNTCognifisense, Inc.K230825Smileyscope System (Therapy Mode)Smileyscope Holding, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.